Canonical Allele Identifier: CA619984551
Gene: NR2F2 HGNC NCBI
NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1180264472
gnomAD v2: 15-96869595-CA-C
gnomAD v3: 15-96326366-CA-C
gnomAD v4: 15-96326366-CA-C
MyVariant Identifiers: chr15:g.96869596del (hg19) chr15:g.96326367del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96326367del , CM000677.2:g.96326367del GRCh38
NC_000015.9:g.96869596del , CM000677.1:g.96869596del GRCh37
NC_000015.8:g.94670600del NCBI36
NG_016753.1:g.5440del

Transcript Alleles

HGVS Amino-acid change
ENST00000421109.6:c.43+15del (NR2F2) ENSP00000401674.2:n.43+15del
NM_001145155.1:c.43+15del (NR2F2) NP_001138627.1:n.43+15del
NR_102743.1:n.163+832del (NR2F2-AS1)
NR_102744.1:n.163+832del (NR2F2-AS1)
NR_125738.1:n.163+589del (NR2F2-AS1)
NM_001145155.2:c.43+15del (NR2F2) NP_001138627.1:n.43+15del
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